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Deuterium N.M.R. relaxation and spectral densities in the discotic mesophase of hexahexyloxytriphenylene

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Zimmermann,  Herbert
Department of Molecular Physics, Max Planck Institute for Medical Research, Max Planck Society;
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;
Zimmermann Group, Max Planck Institute for Medical Research, Max Planck Society;
Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Goldfarb, D., Dong, R. Y., Luz, Z., & Zimmermann, H. (1985). Deuterium N.M.R. relaxation and spectral densities in the discotic mesophase of hexahexyloxytriphenylene. Molecular Physics, 54(5), 1185-1202. doi:10.1080/00268978500100941.


Cite as: https://hdl.handle.net/21.11116/0000-0000-D018-A
Abstract
Longitudinal T 1Z and quadrupolar T 1Q , and transverse T 2 relaxation times of deuterium in all the hydrogen sites of deuterated hexahexyloxytriphenylene (THE6), were measured over the whole stability range of the discotic mesophase. Two isotopic species were used for the measurements, i.e. THE6 deuterated in the aromatic sites, ar d THE6 perdeuterated in the aliphatic chains. Several experimental techniques were used in order to obtain the relaxation times, including the Jeener-Broekaert, selective inversion, and quadrupole echo pulse sequences. Measurements were mainly performed on samples in which the liquid crystalline domains were distributed in a plane with the directors perpendicular to the field direction. Experiments were also made on a single domain sample with the director parallel to the field direction. The experimental results were used to obtain several spectral densities Jp (pω) for both the parallel and perpendicular orientations, of all the deuterium sites in the THE6 molecule. The results are discussed in the light of existing theories.